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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

6-Benzothiazolamine, 2-bromo-

Nc1ccc2c(c1)sc(n2)Br Request for Quotation
Chemical Name: 6-Benzothiazolamine, 2-bromo-
CAS Number: 945400-80-6
Product Number: AG00IIBN(AGN-PC-09MQTG)
Synonyms:
MDL No:
Molecular Formula: C7H5BrN2S
Molecular Weight: 229.0970

Identification/Properties

Computed Properties
Molecular Weight:
229.095g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
227.936g/mol
Monoisotopic Mass:
227.936g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromobenzo[d]thiazol-6-amine is a versatile compound commonly used in chemical synthesis for the preparation of various organic compounds. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it an essential reagent in the pharmaceutical industry for the development of new drugs and bioactive compounds. In chemical synthesis, 2-Bromobenzo[d]thiazol-6-amine can undergo various reactions such as nucleophilic substitution, Suzuki coupling, and palladium-catalyzed cross-coupling reactions to introduce functional groups and create complex molecular structures. Its application in synthesis extends to the construction of heterocyclic compounds, which are important in medicinal chemistry due to their diverse biological activities. Additionally, 2-Bromobenzo[d]thiazol-6-amine plays a crucial role in the preparation of molecular probes, fluorescent dyes, and materials for advanced materials science research.